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Study identifier: NCT07128329 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Acute Effects of Oral Nicotine Pouches

Condition: Nicotine Pouch Self-Administration · Nicotine Pharmacokinetic Study · Nicotine Pharmacodynamic Study  ·  Sponsor: Johns Hopkins University

PhasePhase 1
Planned participants120
Who can joinAll sexes, 21 Years to no upper limit
Healthy volunteersYes

About this study

The present human laboratory study will recruit cigarette smokers (n=60) and adult infrequent nicotine users (n=60) to complete two counterbalanced lab sessions in which the participants use nicotine pouches under controlled conditions. The investigators are recruiting both frequent and infrequent nicotine users because FDA regulates tobacco products based on a public health standard, meaning FDA must consider the impact a regulation may have on the population as a whole (e.g., people who use and do not use tobacco products currently).

This description comes directly from the study's public registry record.

Talk to the study team

Joseph Ciancio, PhD  ·  (410) 550-0529  ·  jcianci3@jh.edu

Lakshmi Kumar, PhD  ·  (410) 550-1928  ·  lkumar6@jh.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Johns Hopkins University School of Medicine, Behavioral Pharmacology Research Unit (Bayview)Baltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07128329